Rosemeire Navickas Constantino-Silva

Author

Also Known As

Maria Luisa Baeza, R. N. Constantino‐Silva, R.N. Constantino-Silva, Rosemeire Constantino-Silva, Rosemeire N. Constantino-Silva, Rosemeire Navickas Constantino-Silva

Publications

368

Citations

H-Index

Concepts

All Affiliations

Faculdade de Medicina do ABC Universidade Federal de São Paulo Universidade Estadual de Campinas (UNICAMP)Universidade de São Paulo Faculdade de Medicina de São José do Rio Preto

About

Rosemeire Navickas Constantino-Silva is an author at Faculdade de Medicina do ABC specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	220
2	Public Health	2	2	31
3	Allergy	1	1	17
4	Immunology	1	1	12
5	Molecular Medicine	1	1	68

Rosemeire Navickas Constantino-Silva

Publications

305

Citations

H-Index

Page 1

	Year	Citations
A Homozygous CARD9 Mutation in a Brazilian Patient with Deep Dermatophytosis Anete Sevciovic Grumach, Flávio Queiroz‐Telles, Mélanie Migaud, Journal of Clinical Immunology Genetic DisorderGeneticsPathologyDeep DermatophytosisMedical Genetics	2015	92
Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families Camila Lopes Veronez, Adriana S. Moreno, Rosemeire Navickas Constantino-Silva, The Journal of Allergy and Clinical Immunology In Practice Hereditary AngioedemaBrazilian FamiliesPathologyF12 MutationsMedicine	2017	68
Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis Pedro Giavina‐Bianchi, L. Karla Arruda, Marcelo Vívolo Aun, Clinics	2018	27
New mutations in SERPING1 gene of Brazilian patients with hereditary angioedema Nathália Cagini, Camila Lopes Veronez, Rosemeire Navickas Constantino-Silva, Biological Chemistry Genetic AnalysisSerping1 GeneNew MutationsAllelic VariantGenetic Disorder	2016	18
The Challenges in the Follow-Up and Treatment of Brazilian Children with Hereditary Angioedema Joanna Araújo-Simões, Aline Gisele Pena Boanova, Rosemeire Navickas Constantino-Silva, International Archives of Allergy and Immunology	2021	18
Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases) N.T.M.L. Fragnan, Alessandra Lima Nogueira Tolentino, Gabriella Borba, Brazilian Journal of Medical and Biological Research AllergyCardiovascular DiseaseAutoimmune DiseaseHereditary AngioedemaHematology	2018	17
Mannose‐binding lectin and MBL‐associated serine protease‐2 gene polymorphisms in a Brazilian population from Rio de Janeiro Natasha Rebouças Ferraroni, Ludovica Segat, Rafael Lima Guimarães, International Journal of Immunogenetics	2011	14
Hereditary Angioedema-Associated Acute Pancreatitis in C1-Inhibitor Deficient and Normal C1-Inhibitor Patients: Case Reports and Literature Review Camila Lopes Veronez, Régis A. Campos, Rosemeire Navickas Constantino-Silva, Frontiers in Medicine	2019	14
Homozygosity for a factor <scp>XII</scp> mutation in one female and one male patient with hereditary angio‐oedema Anete Sevciovic Grumach, C Stieber, Camila Lopes Veronez, Allergy Allelic VariantHereditary Angio-oedemaFactor Xii GeneCardiovascular DiseaseHereditary Angio‐oedema	2015	13
Genetic analysis of hereditary angioedema in a Brazilian family by targeted next generation sequencing Camila Lopes Veronez, Elton Dias da Silva, Patrícia Varela, Biological Chemistry GeneticsImmunologyPathologyDisease Gene IdentificationGenomics	2016	12

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